Filtering package which categorizes and counts how many mutations at a specific location occur within hard clipped reads. Uses a sample's BAM file and RDA file to determine the legitimacy (whether or not a mutation occurs within a hard clipped read) of each mutation within the RDA file. This is done by checking whether any reads in the BAM file contains any reads which occur in the same position and chromosome as a mutation in the RDA file, and which also occurs within a hard clipped region (determined by the CIGAR string of reads from the BAM file)
|Author||L. Christine Schreiner|
|Maintainer||L. Christine Schreiner <[email protected]>|
|Package repository||View on GitHub|
Install the latest version of this package by entering the following in R:
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.